Acatalasemia is a rare genetic disorder characterized by the absence or reduced levels of the enzyme catalase. It can lead to various symptoms including oral ulcerations, gum infections, and skin lesions. The ICD-10 code for Acatalasemia is E80.3. Unfortunately, there is no specific ICD-9 code for Acatalasemia as it was replaced by the ICD-10 coding system. It is important to consult with a healthcare professional for accurate diagnosis and appropriate treatment.
Acatalasemia is a rare genetic disorder characterized by the absence or deficiency of the enzyme catalase, which plays a crucial role in breaking down hydrogen peroxide within cells. This condition leads to the accumulation of hydrogen peroxide, resulting in various health problems.
In terms of medical coding, the International Classification of Diseases, 10th Revision (ICD-10) provides specific codes for acatalasemia. The appropriate ICD-10 code for this condition is D59.8. This code falls under the chapter for "Diseases of the blood and blood-forming organs and certain disorders involving the immune mechanism."
As for the ICD-9 code, it is important to note that the ICD-10 coding system replaced ICD-9 in October 2015. Therefore, acatalasemia does not have a specific ICD-9 code. However, under the old coding system, it may have been classified under a more general code related to enzyme deficiencies or metabolic disorders.
It's essential to consult with a healthcare professional or medical coder for accurate and up-to-date coding information, as they can provide the most precise coding guidance based on the individual patient's situation.